JP2009082383A - Denture stabilizer - Google Patents
Denture stabilizer Download PDFInfo
- Publication number
- JP2009082383A JP2009082383A JP2007255271A JP2007255271A JP2009082383A JP 2009082383 A JP2009082383 A JP 2009082383A JP 2007255271 A JP2007255271 A JP 2007255271A JP 2007255271 A JP2007255271 A JP 2007255271A JP 2009082383 A JP2009082383 A JP 2009082383A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- denture
- salt
- denture stabilizer
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 229960003885 sodium benzoate Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- VXYADVIJALMOEQ-UHFFFAOYSA-K tris(lactato)aluminium Chemical compound CC(O)C(=O)O[Al](OC(=O)C(C)O)OC(=O)C(C)O VXYADVIJALMOEQ-UHFFFAOYSA-K 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C13/00—Dental prostheses; Making same
- A61C13/0025—Linings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/30—Compositions for temporarily or permanently fixing teeth or palates, e.g. primers for dental adhesives
- A61K6/35—Preparations for stabilising dentures in the mouth
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/898—Polysaccharides
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dentistry (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Dental Preparations (AREA)
Abstract
Description
本発明は、義歯床と顎堤の間の隙間に充填して、義歯のガタツキをなくし咀嚼力の低下を改善するために用いられる義歯安定剤に関し、さらに詳しくは、義歯安定剤に必要な粘着性を保持しながらも、チューブ状容器からの出しやすさ、及び使用時の審美性が改善された義歯安定剤に関する。 TECHNICAL FIELD The present invention relates to a denture stabilizer used to fill a gap between a denture base and a ridge and to eliminate the rattle of the denture and to improve the reduction of masticatory force. It is related with the denture stabilizer which improved the ease of taking out from a tube-shaped container and the aesthetics at the time of use, maintaining a property.
従来、義歯安定剤としては、主に酢酸ビニル樹脂からなる非水溶性のペースト状義歯安定剤、鉱物油に水溶性高分子を分散させた水溶性のペースト状義歯安定剤、および、水溶性高分子からなる粉末状義歯安定剤が知られている。 Conventional denture stabilizers include water-insoluble paste denture stabilizers mainly composed of vinyl acetate resin, water-soluble paste denture stabilizers in which water-soluble polymers are dispersed in mineral oil, and water-soluble high denture stabilizers. Powdered denture stabilizers composed of molecules are known.
非水溶性ペースト状義歯安定剤は義歯と口腔粘膜との間にできた隙間を埋めるもので、粘着性は持たないものである。一方、水溶性のペースト状義歯安定剤は唾液に溶解することで粘着性を示すものの、主剤が鉱物油(主にワセリン類、パラフィン類)であるため、口腔内に油系製剤特有の不快感を呈する。また、粉末状義歯安定剤は義歯に塗布する際、粉末が飛び散り、塗布時の操作性が良くない。 The water-insoluble paste denture stabilizer fills the gap formed between the denture and the oral mucosa and does not have adhesiveness. On the other hand, water-soluble paste-like denture stabilizers show adhesiveness when dissolved in saliva, but the main ingredient is mineral oil (mainly petrolatums and paraffins), so there is an unpleasant sensation specific to oil-based preparations in the oral cavity. Presents. In addition, when a powder denture stabilizer is applied to a denture, the powder scatters and the operability during application is not good.
これらの問題を解決する手段として特許文献1では、水または人工唾液と水溶性高分子とグリセリンとからなる義歯安定剤が提案されている。この義歯安定剤は、水溶性のペースト状であってかつ鉱物油を含まないため、油系製剤特有の不快感を呈さないものである。
このような水溶性ペースト状の義歯安定剤は、チューブ状の容器に充填して販売される形態が好ましいと考えられるが、義歯を口腔内で安定化させるために粘着性を向上させると、ペーストが固めになるため、チューブ状の容器から絞り出すことが極めて困難になる。義歯安定剤は比較的高齢者が使用する製品であるため、チューブ状の容器から出しにくいものであると使用時に不都合が生じる。このため、義歯安定剤として必要な粘着性を維持しながらも、ある程度の流動性を保持してチューブ状容器からの出しやすさを確保することが求められる。 It is considered that such a water-soluble paste denture stabilizer is preferably sold in a tube-shaped container. However, in order to stabilize the denture in the oral cavity, the paste is improved. Since it becomes hard, it becomes very difficult to squeeze out from the tubular container. Since denture stabilizers are products used by relatively elderly people, inconvenience arises when they are difficult to remove from a tube-shaped container. For this reason, while maintaining the adhesiveness required as a denture stabilizer, it is requested | required that a certain amount of fluidity | liquidity is hold | maintained and the ease of taking out from a tube-shaped container is ensured.
また、義歯安定剤を用いて義歯を口腔粘膜に貼り付けると義歯と口腔粘膜の隙間から義歯安定剤がはみ出す場合があるが、その場合であっても他者が視認することのできないよう、義歯安定剤が透明なものであることが望ましい。 In addition, if a denture is stuck to the oral mucosa using a denture stabilizer, the denture stabilizer may protrude from the gap between the denture and the oral mucosa. It is desirable that the stabilizer be transparent.
本発明は、上記現状に鑑み、義歯安定剤として必要な粘着性を保持しながらもチューブ状容器からの出しやすさに優れており、さらに高い透明性を有し審美性にも優れた義歯安定剤を提供することを課題とするものである。 In view of the above-mentioned situation, the present invention is excellent in ease of taking out from a tube-like container while maintaining the necessary adhesiveness as a denture stabilizer, and has high transparency and excellent aesthetics. It is an object to provide an agent.
本発明者らは、鋭意検討した結果、セルロース誘導体又はその塩と多価アルコールと水とを含有する義歯安定剤において、セルロース誘導体又はその塩として特定の粘度を持つものを使用し、かつ義歯安定剤が示すちょう度及び粘着力が特定の範囲にあるように調整することによって、上記課題を解決できることを見出し、本発明を完成するに至った。 As a result of intensive studies, the present inventors have used a cellulose derivative or a salt thereof, a polyhydric alcohol and water, and use a cellulose derivative or a salt thereof having a specific viscosity and a denture stable. It has been found that the above problems can be solved by adjusting the consistency and adhesive strength of the agent to be in a specific range, and the present invention has been completed.
すなわち本発明は、2%水溶液の粘度が20〜1500mPa・sのセルロース誘導体又はその塩5〜18重量%と、多価アルコール4〜30重量%と、水とを含有し、且つ、前記セルロース誘導体又はその塩と前記多価アルコールの割合が1:0.5〜1:2.0(重量比)であり、ちょう度が25mm〜38mmであり、粘着力が450g重以上である、ことを特徴とする義歯安定剤に関する。 That is, the present invention includes a cellulose derivative or a salt thereof having a viscosity of 20 to 1500 mPa · s in a 2% aqueous solution, 5 to 18% by weight, 4 to 30% by weight of a polyhydric alcohol, and water, and the cellulose derivative. Or the ratio of the salt and the said polyhydric alcohol is 1: 0.5-1: 2.0 (weight ratio), Consistency is 25 mm-38 mm, Adhesive force is 450 g weight or more, It is characterized by the above-mentioned. It relates to a denture stabilizer.
好ましくは、セルロース誘導体又はその塩の2%水溶液の粘度が20mPa・s以上150mPa・s未満であり、その配合量が13〜17重量%であり、前記多価アルコールの配合量が7.5〜30重量%である。この場合において、水の配合量が53〜79.5重量%であることが好ましい。 Preferably, the viscosity of a 2% aqueous solution of a cellulose derivative or a salt thereof is 20 mPa · s or more and less than 150 mPa · s, the blending amount thereof is 13 to 17% by weight, and the blending amount of the polyhydric alcohol is 7.5 to 30% by weight. In this case, the amount of water is preferably 53 to 79.5% by weight.
また、好ましくは、セルロース誘導体又はその塩の2%水溶液の粘度が150〜1500mPa・sであり、その配合量が6〜10重量%であり、前記多価アルコールの配合量が4〜16重量%である。この場合において、水の配合量が74〜90重量%であることが好ましい。 Preferably, the viscosity of a 2% aqueous solution of a cellulose derivative or a salt thereof is 150 to 1500 mPa · s, the blending amount is 6 to 10% by weight, and the blending amount of the polyhydric alcohol is 4 to 16% by weight. It is. In this case, the amount of water is preferably 74 to 90% by weight.
さらに、好ましくは、セルロース誘導体の塩が、カルボキシメチルセルロースナトリウムである。 Further preferably, the salt of the cellulose derivative is sodium carboxymethyl cellulose.
本発明によると、義歯安定剤として必要な粘着性を保持しながらもチューブ状容器からの出しやすさに優れており、さらに高い透明性を有し審美性にも優れた義歯安定剤を提供することができる。 According to the present invention, there is provided a denture stabilizer that is excellent in ease of taking out from a tube-shaped container while maintaining the necessary adhesiveness as a denture stabilizer, and has high transparency and excellent aesthetics. be able to.
以下に本発明を詳細に説明する。 The present invention is described in detail below.
本発明の義歯安定剤は、必須成分として、セルロース誘導体又はその塩と、多価アルコールと、水とを含有する水性の製剤であり、水溶性で、かつペースト状を呈するものである。 The denture stabilizer of the present invention is an aqueous preparation containing a cellulose derivative or a salt thereof, a polyhydric alcohol, and water as essential components, and is water-soluble and exhibits a paste form.
セルロース誘導体又はその塩は水に溶解又はゲル化して粘着性を生じさせるものであり、2%水溶液の粘度が20〜1500mPa・sの範囲にあるものを使用する。なお、この2%水溶液粘度は、2%水溶液を作製し、25℃となるように調整をした後、BM型粘度計にて計測したものである。セルロース誘導体又はその塩の2%水溶液粘度が20mPa・s未満であると、義歯安定剤がペースト状を保ち得ず、また、十分な粘着力を確保することができない。逆に1500mPa・sを超えた場合には、製剤が固くなりすぎ、チューブ状容器から出しにくくなるとともに、製剤に濁りが生じ十分な透明性を達成することが困難になる。なお、特定の粘度を有するセルロース誘導体又はその塩は広く市販されており、本発明ではこれを利用することができる。 A cellulose derivative or a salt thereof is dissolved or gelled in water to cause stickiness, and a 2% aqueous solution having a viscosity of 20 to 1500 mPa · s is used. The viscosity of this 2% aqueous solution was measured with a BM viscometer after preparing a 2% aqueous solution and adjusting it to 25 ° C. If the viscosity of the 2% aqueous solution of the cellulose derivative or salt thereof is less than 20 mPa · s, the denture stabilizer cannot maintain the paste form, and sufficient adhesive strength cannot be ensured. On the other hand, when it exceeds 1500 mPa · s, the preparation becomes too hard and difficult to take out from the tube-like container, and the preparation becomes cloudy and it becomes difficult to achieve sufficient transparency. In addition, the cellulose derivative or its salt which has specific viscosity is widely marketed, and can utilize this in this invention.
セルロース誘導体又はその塩の種類としては特に限定されないが、例えば、水溶性のセルロースエーテルであるアルキルセルロース(例えばメチルセルロース、エチルセルロース等)、ヒドロキシ化されたアルキルセルロース(例えばヒドロキシプロピルメチルセルロース、ヒドロキシエチルセルロース等)、アルカリ金属カルボキシメチルセルロース(例えばカルボキシメチルセルロースナトリウム、カルボキシメチルセルロースカリウム等)、アルカリ金属セルロース硫酸塩等が挙げられる。これらのうち1種類のみを使用してもよいし、複数種を併用してもよい。なかでも、膨潤又はゲル化性能や、粘着性が高いことから、カルボキシメチルセルロースナトリウムが好ましい。 Although it does not specifically limit as a kind of cellulose derivative or its salt, For example, alkyl cellulose (for example, methylcellulose, ethylcellulose, etc.) which is water-soluble cellulose ether, Hydroxylated alkylcellulose (for example, hydroxypropylmethylcellulose, hydroxyethylcellulose, etc.), Examples include alkali metal carboxymethyl cellulose (for example, sodium carboxymethyl cellulose, potassium carboxymethyl cellulose), alkali metal cellulose sulfate and the like. Of these, only one type may be used, or a plurality of types may be used in combination. Of these, sodium carboxymethylcellulose is preferred because of its swelling or gelling performance and high adhesiveness.
多価アルコールはセルロース誘導体又はその塩及び水と共存することによって製剤の粘着性を高める成分であり、アルコール性水酸基を2個以上有する化合物であれば特に限定されない。具体的には、グリセリン、プロピレングリコール、ソルビトール、ポリエチレングリコール等が挙げられるが、これらのうち1種類のみを使用してもよいし、複数種を併用してもよい。なかでも、粘着性やちょう度の観点から、グリセリンが好ましい。 A polyhydric alcohol is a component which improves the adhesiveness of a formulation by coexisting with a cellulose derivative or a salt thereof and water, and is not particularly limited as long as it is a compound having two or more alcoholic hydroxyl groups. Specific examples include glycerin, propylene glycol, sorbitol, polyethylene glycol, and the like. Of these, only one type may be used, or a plurality of types may be used in combination. Among these, glycerin is preferable from the viewpoints of tackiness and consistency.
さらに本発明の義歯安定剤は、水を含有するが、使用できる水としては、通常の精製水のほか、人工唾液であってもよい。これを配合することによって、水溶性のペースト状製剤とすることができる。 Furthermore, the denture stabilizer of the present invention contains water, but the water that can be used may be normal purified water or artificial saliva. By blending this, a water-soluble paste-form preparation can be obtained.
本発明の義歯安定剤においてセルロース誘導体又はその塩の配合量は5〜18重量%の範囲にあり、多価アルコールの配合量は4〜30重量%の範囲にある。残量は、後述する任意の添加剤を除外すると水が占める。さらにセルロース誘導体又はその塩と多価アルコールは、重量比で1:0.5〜1:2.0を満足する範囲で使用される。セルロース誘導体又はその塩の配合量が少なすぎると、義歯安定剤がペースト状にならず、十分な粘着性を示すことができないので、義歯を口腔内に安定性よく維持することができない。逆にその配合量が多すぎると、製剤が固くなることによってチューブ状容器から出しにくくなり、また、十分な透明感を達成することが困難になる。 In the denture stabilizer of the present invention, the blending amount of the cellulose derivative or a salt thereof is in the range of 5 to 18% by weight, and the blending amount of the polyhydric alcohol is in the range of 4 to 30% by weight. The remaining amount is occupied by water excluding any additives described later. Further, the cellulose derivative or a salt thereof and the polyhydric alcohol are used in a range satisfying 1: 0.5 to 1: 2.0 by weight ratio. When the blending amount of the cellulose derivative or its salt is too small, the denture stabilizer does not become a paste and cannot exhibit sufficient adhesiveness, so that the denture cannot be stably maintained in the oral cavity. On the other hand, when the blending amount is too large, it becomes difficult to take out the tube-like container due to the hardened preparation, and it becomes difficult to achieve sufficient transparency.
本発明の義歯安定剤は、ちょう度が25mm〜38mmの範囲にあり、かつ粘着力が450g重以上のものである。以上の範囲を満足することによって、義歯安定剤に必要な粘着性と、チューブ状容器からの出しやすさとを両立し、さらに製剤の透明性を確保することが可能になる。粘着力は700g重以上が好ましく、1000g重以上が特に好ましい。上限としてはおよそ2000g重以下のものを好適に使用することができる。 The denture stabilizer of the present invention has a consistency of 25 mm to 38 mm and an adhesive strength of 450 g weight or more. By satisfying the above range, it is possible to achieve both the adhesiveness necessary for the denture stabilizer and the ease of taking out from the tube-shaped container, and further ensure the transparency of the preparation. The adhesive strength is preferably 700 g weight or more, particularly preferably 1000 g weight or more. As an upper limit, about 2000 g weight or less can be used conveniently.
以上のようなちょう度と粘着力の関係を満足する義歯安定剤を得るには、配合するセルロース誘導体又はその塩が示す2%水溶液粘度と、その配合量、多価アルコールの配合量、及び両者の割合を本発明の範囲内において適宜調整すればよい。 In order to obtain a denture stabilizer that satisfies the above-mentioned relationship between consistency and adhesive strength, the 2% aqueous solution viscosity of the cellulose derivative or salt thereof to be blended, its blending amount, the blending amount of the polyhydric alcohol, and both The ratio may be adjusted as appropriate within the scope of the present invention.
その調整方法については後述する実施例と比較例を対比することによって容易に理解可能であるが、全般的な傾向として、2%水溶液粘度が低めのセルロース誘導体又はその塩を用いる場合には、その配合量や多価アルコールの配合量は多いほうが望ましく、逆に2%水溶液粘度が高めのセルロース誘導体又はその塩を用いる場合にはその配合量や多価アルコールの配合量は少ないほうが望ましい。 The adjustment method can be easily understood by comparing Examples and Comparative Examples described later, but as a general tendency, when using a cellulose derivative or a salt thereof having a low 2% aqueous solution viscosity, It is desirable that the blending amount and the blending amount of the polyhydric alcohol are large. Conversely, when a cellulose derivative having a high 2% aqueous solution viscosity or a salt thereof is used, it is desirable that the blending amount or the blending amount of the polyhydric alcohol is small.
このような傾向を満足する具体的な一態様としては、セルロース誘導体又はその塩の2%水溶液の粘度が20mPa・s以上150mPa・s未満である場合には、その配合量が13〜17重量%であり、多価アルコールの配合量が7.5〜30重量%である。この際、水の配合量としては53〜79.5重量%であることが好ましい。 As a specific embodiment satisfying such a tendency, when the viscosity of a 2% aqueous solution of a cellulose derivative or a salt thereof is 20 mPa · s or more and less than 150 mPa · s, the blending amount is 13 to 17% by weight. The blending amount of the polyhydric alcohol is 7.5 to 30% by weight. At this time, the blending amount of water is preferably 53 to 79.5% by weight.
また、別の態様としては、セルロース誘導体又はその塩の2%水溶液の粘度が150〜1500mPa・sである場合には、その配合量が6〜10重量%であり、前記多価アルコールの配合量が4〜16重量%である。この際、水の配合量としては74〜90重量%であることが好ましい。 As another aspect, when the viscosity of a 2% aqueous solution of a cellulose derivative or a salt thereof is 150 to 1500 mPa · s, the blending amount is 6 to 10% by weight, and the blending amount of the polyhydric alcohol Is 4 to 16% by weight. At this time, the amount of water is preferably 74 to 90% by weight.
本発明の義歯安定剤には、上記成分以外に、義歯安定剤に所望の性状を与えるために可塑剤、乳化剤、粘度調整剤、水不溶性粉体、防腐剤、金属石けん、溶剤、可溶化剤、安定化剤、消臭剤、機能性成分、酵素、清涼剤、香料、着色料など公知の添加剤を本発明の効果を損なわない限りにおいて、適宜配合してもよい。 In addition to the above components, the denture stabilizer of the present invention includes a plasticizer, an emulsifier, a viscosity modifier, a water-insoluble powder, an antiseptic, a metal soap, a solvent, and a solubilizer in order to give the denture stabilizer the desired properties. As long as the effects of the present invention are not impaired, known additives such as stabilizers, deodorants, functional ingredients, enzymes, refreshing agents, fragrances, and coloring agents may be appropriately blended.
可塑剤としては、ミツロウ、木ロウ、カルナウバロウ、キャンデリラワックスが例示される。 Examples of the plasticizer include beeswax, wood wax, carnauba wax, and candelilla wax.
乳化剤としては、グリセリンモノステアレートのようなグリセリンの脂肪酸エステル、ソルビタンモノステアレートのようなソルビタンの脂肪酸エステル、ステアリン酸スクロース、ラウリン酸スクロースのようなショ糖脂肪酸エステルが例示される。 Examples of emulsifiers include glycerin fatty acid esters such as glycerin monostearate, sorbitan fatty acid esters such as sorbitan monostearate, and sucrose fatty acid esters such as sucrose stearate and sucrose laurate.
水不溶性粉体としては、炭酸カルシウム、リン酸カルシウム、プラスチックパウダー、タルク、シリカ、ベントナイト、ゼオライト等が例示される。 Examples of the water-insoluble powder include calcium carbonate, calcium phosphate, plastic powder, talc, silica, bentonite, and zeolite.
防腐剤としては、安息香酸、安息香酸ナトリウム、メチルパラベン、エチルパラベン、プロピルパラベンが例示される。 Examples of the preservative include benzoic acid, sodium benzoate, methyl paraben, ethyl paraben, and propyl paraben.
金属石けんとしては、ステアリン酸カルシウムが例示される。 An example of the metal soap is calcium stearate.
溶剤としては、フェノキシエタノールが例示される。 An example of the solvent is phenoxyethanol.
可溶化剤としては、ポリオキシエチレン硬化ヒマシ油、モノオレイン酸ポリエチレングリコールのようなポリオキシエチレン脂肪酸エステル、N−ラウロイルサルコシンナトリウムのようなN−アシルアミノ酸塩、ラウリルジメチルアミノ酢酸ベタインのようなアルキル(アミド)ベタイン、ポリオキシエチレンラウリルエーテルのようなポリオキシアルキレンラウリルエーテル、ポリオキシエチレンアルキルエーテル、ヤシ油脂肪酸モノエタノールアミドのようなアルキルアルカノールアミド等が例示される。 Examples of solubilizers include polyoxyethylene hydrogenated castor oil, polyoxyethylene fatty acid esters such as polyethylene glycol monooleate, N-acyl amino acid salts such as sodium N-lauroyl sarcosine, and alkyls such as lauryldimethylaminoacetic acid betaine. Examples include (amide) betaines, polyoxyalkylene lauryl ethers such as polyoxyethylene lauryl ether, polyoxyethylene alkyl ethers, alkyl alkanol amides such as coconut oil fatty acid monoethanolamide, and the like.
安定化剤としては、酸化チタン、塩化ナトリウム、塩化カリウム、塩化マグネシウム、乳酸アルミニウム等が例示される。 Examples of the stabilizer include titanium oxide, sodium chloride, potassium chloride, magnesium chloride, aluminum lactate and the like.
消臭剤としては、銅クロロフィリンナトリウム、コーヒー、緑茶、ブドウ等から抽出されるポリフェノール類等が例示される。 Examples of the deodorant include polyphenols extracted from copper chlorophyllin sodium, coffee, green tea, grapes and the like.
機能性成分としては、グリチルレチン酸、グリチルレチン酸塩、グリチルリチン酸、グリチルリチン酸塩のような抗炎症剤、イソプロピルメチルフェノール、トリクロサン、塩化セチルピリジニウム、塩化デカリニウム、塩化ベンゼトニウム、塩化ベンザルコニウム、クロルヘキシジン類、ヒノキチオールのような殺菌剤、抗生物質、アスコルビン酸、アスコルビン酸誘導体、酢酸トコフェロール等のビタミン類等が例示される。 As functional components, anti-inflammatory agents such as glycyrrhetinic acid, glycyrrhetinic acid salt, glycyrrhizic acid, glycyrrhizinate, isopropylmethylphenol, triclosan, cetylpyridinium chloride, decalinium chloride, benzethonium chloride, benzalkonium chloride, chlorhexidines, Examples include bactericides such as hinokitiol, antibiotics, ascorbic acid, ascorbic acid derivatives, vitamins such as tocopherol acetate, and the like.
酵素としては、デキストラナーゼ、アミラーゼ、プロテアーゼ、ムタナーゼ、溶菌酵素、リゾチーム等が例示される。 Examples of the enzyme include dextranase, amylase, protease, mutanase, lytic enzyme, lysozyme and the like.
清涼剤としては、l−メントール、dl−メントール、メントール誘導体、カルボン等が例示される。 Examples of the refreshing agent include l-menthol, dl-menthol, menthol derivatives, carvone and the like.
また、口腔内での義歯安定剤の唾液への溶解性を低下させ同剤が徐々に溶け出すようにするためにナトリウム/カルシウム・メトキシエチレン無水マレイン酸共重合体塩を添加することも好ましい。 It is also preferable to add a sodium / calcium methoxyethylene maleic anhydride copolymer salt in order to reduce the solubility of the denture stabilizer in the oral cavity in the oral cavity and gradually dissolve the agent.
本発明による義歯安定剤を製造するには、例えば、水、多価アルコール、及びセルロース誘導体又はその塩を混合し、水にセルロース誘導体又はその塩を溶解又はゲル化させることによって、水溶性ペーストとすればよい。 In order to produce the denture stabilizer according to the present invention, for example, water, a polyhydric alcohol, and a cellulose derivative or a salt thereof are mixed, and the cellulose derivative or a salt thereof is dissolved or gelled in water, thereby do it.
本発明の義歯安定剤は、チューブ状の容器に充填することによって、保存中の配合成分の揮発や外来物の混入等を防止することができる。本発明の義歯安定剤はチューブ状容器からの出しやすさに優れているから、たとえ使用者が高齢者の場合であってもチューブ状容器から容易に絞り出すことができる。本発明の義歯安定剤を充填することが可能なチューブ状容器としては特に限定されないが、例えば、アルミニウム製チューブ、アルミニウム・エポキシフェノール樹脂製多層チューブ、アルミニウム・ポリエチレン製多層チューブ、アルミニウム・ポリエチレン・エポキシフェノール樹脂製多層チューブ等のアルミラミネートチューブ等が挙げられる。 By filling the denture stabilizer of the present invention in a tube-shaped container, it is possible to prevent volatilization of the blended components during storage, mixing of foreign substances, and the like. Since the denture stabilizer of this invention is excellent in the ease of taking out from a tube-shaped container, even if a user is an elderly person, it can squeeze out from a tube-shaped container easily. Although it does not specifically limit as a tube-shaped container which can be filled with the denture stabilizer of this invention, For example, the tube made from aluminum, the multilayer tube made from an aluminum epoxy phenol resin, the multilayer tube made from aluminum polyethylene, an aluminum polyethylene polyethylene epoxy An aluminum laminate tube such as a phenol resin multilayer tube may be used.
以下に実施例を掲げて本発明を詳細に説明するが、本発明はこれら実施例に限定されるものではない。
実施例1〜7及び比較例1〜8
表1に示す2%水溶液粘度を有するカルボキシメチルセルロースナトリウム、グリセリン、及び精製水を表1に示す重量%で混合し、十分に攪拌することによって前記セルロースを水に溶解又はゲル化させて、水溶性ペースト状の義歯安定剤を製造した。
EXAMPLES The present invention will be described in detail below with reference to examples, but the present invention is not limited to these examples.
Examples 1-7 and Comparative Examples 1-8
Mixing sodium carboxymethylcellulose having a 2% aqueous solution viscosity shown in Table 1, glycerin, and purified water at a weight percentage shown in Table 1, and sufficiently stirring the cellulose to dissolve or gel the water, thereby being water-soluble. A pasty denture stabilizer was produced.
得られた義歯安定剤を、次の項目に従って評価した。得られた結果を表1に示す。
a)粘着力
得られた義歯安定剤について、JIS−T−6525−1 粘着力試験Iの試験方法にて塗布1分後の粘着力を計測した。得られた数値が450g重以上である場合は○と判定し、450g重に満たない場合を×と判定した。
b)ちょう度
得られた義歯安定剤について、JIS−T−6525−2 ちょう度の試験方法にてちょう度を計測した。得られた数値が25〜38mmの範囲内にある場合は○と判定し、この範囲にない場合は×と判定した。
c)出しやすさ
得られた義歯安定剤をアルミラミネートチューブに充填した後、試験者がチューブに力を加えて義歯安定剤を絞り出す際に、その出しやすさを、以下の評価基準に基づいて体感で判定した。
○:容易に搾り出せる
△:搾り出せる
×:硬くて搾り出せない
××:軟らかすぎてチューブから溢れる
d)透明感
得られた義歯安定剤について目視によりその透明性を評価した。
○:透明である。
△:濁りが見られ、透明性が十分ではない。
The obtained denture stabilizer was evaluated according to the following items. The obtained results are shown in Table 1.
a) Adhesive strength About the obtained denture stabilizer, the adhesive strength 1 minute after application | coating was measured by the test method of JIS-T-6525-1 adhesive strength test I. When the obtained numerical value was 450 g weight or more, it was determined as ◯, and when it was less than 450 g weight, it was determined as x.
b) Consistency About the obtained denture stabilizer, the consistency was measured by the test method of JIS-T-6525-2 consistency. When the obtained numerical value was within the range of 25 to 38 mm, it was determined as “good”, and when it was not within this range, it was determined as “poor”.
c) Ease of taking out After filling the obtained denture stabilizer in an aluminum laminate tube, when the tester applies force to the tube to squeeze out the denture stabilizer, the easiness of taking out is based on the following evaluation criteria. Judgment was based on experience.
○: Can be easily squeezed Δ: Can be squeezed ×: Hard and cannot be squeezed XX: Too soft and overflowing from the tube d) Transparency The obtained denture stabilizer was visually evaluated.
○: Transparent.
(Triangle | delta): Turbidity is seen and transparency is not enough.
Claims (6)
前記セルロース誘導体又はその塩と前記多価アルコールの割合が1:0.5〜1:2.0(重量比)であり、
ちょう度が25mm〜38mmであり、
粘着力が450g重以上である、ことを特徴とする義歯安定剤。 A 2% aqueous solution having a viscosity of 20 to 1500 mPa · s, a cellulose derivative or a salt thereof, 5 to 18% by weight, a polyhydric alcohol 4 to 30% by weight, water, and
The ratio of the cellulose derivative or salt thereof and the polyhydric alcohol is 1: 0.5 to 1: 2.0 (weight ratio),
The consistency is 25 mm to 38 mm,
A denture stabilizer characterized by having an adhesive strength of 450 g weight or more.
The denture stabilizer in any one of Claims 1-5 whose salt of a cellulose derivative is carboxymethylcellulose sodium.
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JPS5799511A (en) * | 1980-12-13 | 1982-06-21 | Lion Corp | Denture stabilizing agent |
JP3515761B2 (en) * | 2001-02-02 | 2004-04-05 | 恬男 日野 | Oral moisturizer for dentures |
JP2004352612A (en) * | 2003-03-31 | 2004-12-16 | Kobayashi Pharmaceut Co Ltd | Artificial tooth stabilizer |
JP2007097718A (en) * | 2005-09-30 | 2007-04-19 | Kobayashi Pharmaceut Co Ltd | Denture fixing agent |
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JPS5799511A (en) * | 1980-12-13 | 1982-06-21 | Lion Corp | Denture stabilizing agent |
JP3515761B2 (en) * | 2001-02-02 | 2004-04-05 | 恬男 日野 | Oral moisturizer for dentures |
JP2004352612A (en) * | 2003-03-31 | 2004-12-16 | Kobayashi Pharmaceut Co Ltd | Artificial tooth stabilizer |
JP2007097718A (en) * | 2005-09-30 | 2007-04-19 | Kobayashi Pharmaceut Co Ltd | Denture fixing agent |
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